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OpenTrials
Completed

NCT Number: NCT01330004

Blood Pressure Change and Outcome

Hyper- and hypotension are important predictors of survival in non-ESRD (end stage renal disease) population. In dialysis patients, however, it has been shown that higher blood pressure levels may actually be beneficial to patient outcomes. Dynamics of blood pressure evolution over time has not been previously studied in dialysis population. The investigators aim to understand how both blood pressure levels and blood pressure changes over time predict patient survival.

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Key information

Age range

18 year–88 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Renal Research Institute

New York, 10128, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Hemodialysis

Treatment and study plan

Primary outcomes

  1. Effect size of the relation of dynamic changes of blood pressure (BP) at different ranges of BP to survival in incident hemodialysis patients.

    Time frame: Up to 11 years and 11 months

    The ranges of blood pressure measurements in mmHg over time and the relation to patient outcomes (including survival)

Sponsors and collaborators

Lead sponsor

Renal Research Institute

Other

Registry information

Official study title

The Relationship of Systolic and Diastolic Blood Pressure Changes Over Time to Patient Outcomes in Incident Hemodialysis Patients

Acronym: BP

Important dates

Study start
1999
Primary completion
2010
Study completion
2010
First posted
Apr 6, 2011
Registry last updated
May 5, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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